Variant report
| Variant | rs7988749 |
|---|---|
| Chromosome Location | chr13:61694949-61694950 |
| allele | C/T |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:1 , 50 per page) page:
1
| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr13:61229131..61230781-chr13:61693406..61695295,2 | MCF-7 | breast: |
| No data |
| No data |
| No data |
| No data |
rSNPs within LD-proxies of this variant (count:20)
| rs_ID | r2[population] |
|---|---|
| rs12583135 | 0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes] |
| rs12584190 | 0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes] |
| rs1319682 | 0.85[AMR][1000 genomes];0.86[ASN][1000 genomes] |
| rs1355961 | 0.85[AMR][1000 genomes];0.84[ASN][1000 genomes] |
| rs2323083 | 0.85[AMR][1000 genomes];0.86[ASN][1000 genomes] |
| rs28769373 | 0.85[AMR][1000 genomes];0.86[ASN][1000 genomes] |
| rs3900232 | 0.85[AMR][1000 genomes];0.86[ASN][1000 genomes] |
| rs58201207 | 0.85[AMR][1000 genomes];0.86[ASN][1000 genomes] |
| rs7991819 | 0.85[AMR][1000 genomes];0.86[ASN][1000 genomes] |
| rs7991828 | 0.85[AMR][1000 genomes];0.86[ASN][1000 genomes] |
| rs7997758 | 0.81[EUR][1000 genomes];0.81[ASN][1000 genomes] |
| rs7997806 | 0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes] |
| rs9563871 | 0.85[AMR][1000 genomes];0.86[ASN][1000 genomes] |
| rs9563872 | 0.85[AMR][1000 genomes];0.86[ASN][1000 genomes] |
| rs9563873 | 0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes] |
| rs9563874 | 0.97[EUR][1000 genomes];0.86[ASN][1000 genomes] |
| rs9563875 | 0.97[EUR][1000 genomes];0.86[ASN][1000 genomes] |
| rs9570462 | 0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.86[ASN][1000 genomes] |
| rs9570470 | 0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes] |
| rs9570502 | 0.82[MEX][hapmap] |
Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv832626 | chr13:61545191-61698233 | Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Strong transcription | Chromatin interactive regionlncRNA | 1 gene(s) | inside rSNPs | diseases |
| 2 | nsv832627 | chr13:61642811-61829217 | Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 1 gene(s) | inside rSNPs | diseases |
| 3 | esv3444432 | chr13:61665252-61781081 | Enhancers Strong transcription Weak transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 1 gene(s) | inside rSNPs | diseases |
| No data |
| No. | Chromosome Location | Chromatin state | Cell line | Tissue |
|---|---|---|---|---|
| 1 | chr13:61694400-61699800 | Weak transcription | hESC Derived CD184+ Endoderm Cultured Cells | ES cell derived |
